| Literature DB >> 32139446 |
Abubakar Sharif1, Lucinda Carr2, Efstratios Saliakellis3, Himadri Chakraborty4.
Abstract
We present a case of Sandifer syndrome in a 3-year-old girl who initially presented with a history of recurrent paroxysmal head drops associated with ataxia-like symptoms and recurrent falls sustaining a clavicular fracture on one occasion. She was referred to and seen by the paediatric neurologist. Physical examination, electroencephalogram, MRI brain, electromyograph single fibre study and blood tests were all normal. With the history of hiccups and choking-like episodes she was referred to the speech and language therapist (SALT). SALT assessment did not reveal indications of swallowing impairment or possible aspiration. A barium swallow later showed small amount of reflux into the distal oesophagus. This prompted a trial of lansoprazole and she was referral to the gastroenterologists. Endoscopy and oesophageal manometry were essentially normal. However, the pH impedance study revealed severe gastro-oesophageal reflux disease. She continued with lansoprazole and dairy-free diet and her symptoms resolved. © BMJ Publishing Group Limited 2020. No commercial re-use. See rights and permissions. Published by BMJ.Entities:
Keywords: clinical neurophysiology; epilepsy and seizures; gastro-oesophageal reflux; movement disorders (other than Parkinsons); neurogastroenterology
Mesh:
Substances:
Year: 2020 PMID: 32139446 PMCID: PMC7059500 DOI: 10.1136/bcr-2019-230989
Source DB: PubMed Journal: BMJ Case Rep ISSN: 1757-790X